FDA Recall United States Terminated Historical recordClass I
Almark Foods, LLC
- Product
- White Medium Hard Cooked Eggs sold under the brand names of:…
- Published
- February 12, 2020
- Distribution
- Product was shipped to the following sta…
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Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass I
The firm was notified by FDA & CDC of a potential Listeria monocytogenes genetic match between environmental samples from our facility and case patient samples associated with an illness outbreak.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Almark Foods Smokehouse ProBox Cage Free Hard Cooked Eggs | Not published in this source record | 628,531 retail packages of various sizes (total) | All lot codes containing "G" with a USED BY DATE on or before 11/2020 |
This recall shares FDA event ID 84543 with 9 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
Responsible company: Almark Foods, LLC
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Alabama | 1 |
| Arkansas | 1 |
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Connecticut | 1 |
| District of Columbia | 1 |
| Florida | 1 |
| Georgia | 1 |
| Iowa | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kansas | 1 |
| Kentucky | 1 |
| Louisiana | 1 |
| Massachusetts | 1 |
| Maryland | 1 |
| Maine | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| Mississippi | 1 |
| North Carolina | 1 |
| North Dakota | 1 |
| New Hampshire | 1 |
| New Jersey | 1 |
| Nevada | 1 |
| New York | 1 |
| Ohio | 1 |
| Oklahoma | 1 |
| Oregon | 1 |
| Pennsylvania | 1 |
| South Carolina | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Utah | 1 |
| Virginia | 1 |
| Washington | 1 |
| Wisconsin | 1 |
| Wyoming | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
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